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Iron in PDB 1b0p: Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus

Enzymatic activity of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus

All present enzymatic activity of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus:
1.2.7.1;

Protein crystallography data

The structure of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus, PDB code: 1b0p was solved by E.Chabriere, M.H.Charon, A.Volbeda, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 6.00 / 2.31
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 84.800, 144.900, 203.000, 90.00, 90.00, 90.00
R / Rfree (%) 19.9 / 27.1

Other elements in 1b0p:

The structure of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus also contains other interesting chemical elements:

Magnesium (Mg) 2 atoms
Calcium (Ca) 2 atoms

Iron Binding Sites:

Pages:

>>> Page 1 <<< Page 2, Binding sites: 11 - 20; Page 3, Binding sites: 21 - 24;

Binding sites:

The binding sites of Iron atom in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus (pdb code 1b0p). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 24 binding sites of Iron where determined in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus, PDB code: 1b0p:
Jump to Iron binding site number: 1; 2; 3; 4; 5; 6; 7; 8; 9; 10;

Iron binding site 1 out of 24 in 1b0p

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Iron binding site 1 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1233

b:8.6
occ:1.00
FE1 A:SF41233 0.0 8.6 1.0
S2 A:SF41233 2.3 5.6 1.0
S3 A:SF41233 2.3 5.5 1.0
S4 A:SF41233 2.3 5.3 1.0
SG A:CYS689 2.3 6.7 1.0
FE3 A:SF41233 2.6 5.0 1.0
FE2 A:SF41233 2.6 8.1 1.0
FE4 A:SF41233 2.7 3.6 1.0
CB A:CYS689 3.5 7.4 1.0
CA A:CYS689 3.9 7.3 1.0
S1 A:SF41233 3.9 5.7 1.0
CB A:ALA761 4.0 5.4 1.0
N A:ILE690 4.0 6.7 1.0
NE1 A:TRP684 4.0 3.2 1.0
N A:GLN691 4.0 5.2 1.0
C A:CYS689 4.4 7.2 1.0
CG1 A:ILE738 4.4 2.0 1.0
N A:CYS692 4.4 5.6 1.0
CA A:GLN691 4.5 5.6 1.0
SG A:CYS755 4.7 4.1 1.0
CD1 A:TRP684 4.8 3.0 1.0
SG A:CYS695 4.8 5.2 1.0
SG A:CYS692 4.9 5.2 1.0
C A:ILE690 4.9 5.3 1.0

Iron binding site 2 out of 24 in 1b0p

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Iron binding site 2 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1233

b:8.1
occ:1.00
FE2 A:SF41233 0.0 8.1 1.0
S1 A:SF41233 2.3 5.7 1.0
S3 A:SF41233 2.3 5.5 1.0
S4 A:SF41233 2.3 5.3 1.0
SG A:CYS692 2.3 5.2 1.0
FE3 A:SF41233 2.6 5.0 1.0
FE1 A:SF41233 2.6 8.6 1.0
FE4 A:SF41233 2.7 3.6 1.0
N A:CYS692 3.5 5.6 1.0
CB A:CYS692 3.5 6.2 1.0
CD A:PRO756 3.8 6.1 1.0
S2 A:SF41233 3.9 5.6 1.0
CA A:CYS692 3.9 5.4 1.0
N A:ASN693 4.0 4.5 1.0
C A:CYS692 4.3 5.2 1.0
N A:GLN694 4.3 3.5 1.0
CG1 A:ILE690 4.3 4.9 1.0
N A:GLN691 4.6 5.2 1.0
C A:GLN691 4.7 5.8 1.0
SG A:CYS689 4.7 6.7 1.0
SG A:CYS695 4.7 5.2 1.0
CG A:PRO756 4.7 6.2 1.0
N A:CYS695 4.8 3.5 1.0
SG A:CYS755 4.8 4.1 1.0
CB A:GLN694 4.8 3.0 1.0
N A:ILE690 4.9 6.7 1.0
CA A:ASN693 4.9 3.8 1.0
CA A:GLN691 5.0 5.6 1.0
N A:PRO756 5.0 6.5 1.0

Iron binding site 3 out of 24 in 1b0p

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Iron binding site 3 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1233

b:5.0
occ:1.00
FE3 A:SF41233 0.0 5.0 1.0
S4 A:SF41233 2.3 5.3 1.0
S2 A:SF41233 2.3 5.6 1.0
SG A:CYS695 2.4 5.2 1.0
S1 A:SF41233 2.4 5.7 1.0
FE1 A:SF41233 2.6 8.6 1.0
FE2 A:SF41233 2.6 8.1 1.0
FE4 A:SF41233 2.7 3.6 1.0
CB A:CYS695 3.3 4.8 1.0
S3 A:SF41233 3.8 5.5 1.0
N A:CYS695 3.9 3.5 1.0
CG1 A:ILE738 4.0 2.0 1.0
CA A:CYS695 4.2 3.7 1.0
CD1 A:ILE738 4.3 2.0 1.0
N A:ASN693 4.5 4.5 1.0
SG A:CYS692 4.6 5.2 1.0
SG A:CYS689 4.6 6.7 1.0
N A:GLN694 4.7 3.5 1.0
CA A:ASN693 4.8 3.8 1.0
SG A:CYS755 4.8 4.1 1.0
CD1 A:LEU762 4.9 2.0 1.0
CG2 A:ILE738 4.9 2.6 1.0
CB A:ILE738 5.0 3.5 1.0

Iron binding site 4 out of 24 in 1b0p

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Iron binding site 4 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1233

b:3.6
occ:1.00
FE4 A:SF41233 0.0 3.6 1.0
S3 A:SF41233 2.3 5.5 1.0
S1 A:SF41233 2.3 5.7 1.0
S2 A:SF41233 2.3 5.6 1.0
SG A:CYS755 2.3 4.1 1.0
FE3 A:SF41233 2.7 5.0 1.0
FE1 A:SF41233 2.7 8.6 1.0
FE2 A:SF41233 2.7 8.1 1.0
CB A:CYS755 3.4 4.5 1.0
CB A:ALA761 3.5 5.4 1.0
CA A:CYS755 3.7 4.8 1.0
S4 A:SF41233 4.0 5.3 1.0
CD A:PRO756 4.0 6.1 1.0
C A:CYS755 4.4 5.7 1.0
N A:PRO756 4.4 6.5 1.0
CD A:PRO757 4.5 10.4 1.0
CA A:ALA761 4.6 5.8 1.0
CG A:LEU762 4.6 2.0 1.0
SG A:CYS692 4.7 5.2 1.0
SG A:CYS695 4.8 5.2 1.0
N A:ALA761 4.8 7.4 1.0
SG A:CYS689 4.9 6.7 1.0
C A:ALA761 4.9 5.3 1.0
CD1 A:LEU762 4.9 2.0 1.0
N A:CYS755 4.9 4.7 1.0
CB A:CYS695 4.9 4.8 1.0
CG A:PRO757 4.9 10.8 1.0

Iron binding site 5 out of 24 in 1b0p

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Iron binding site 5 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 5 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1234

b:3.8
occ:1.00
FE1 A:SF41234 0.0 3.8 1.0
S2 A:SF41234 2.2 3.5 1.0
SG A:CYS699 2.2 2.6 1.0
S4 A:SF41234 2.3 3.3 1.0
S3 A:SF41234 2.4 4.4 1.0
FE4 A:SF41234 2.6 2.2 1.0
FE3 A:SF41234 2.7 4.0 1.0
FE2 A:SF41234 2.7 2.0 1.0
CB A:CYS699 3.3 2.0 1.0
CA A:CYS699 3.8 2.6 1.0
S1 A:SF41234 3.9 2.6 1.0
CD A:PRO700 4.0 2.0 1.0
CB A:ALA703 4.0 2.3 1.0
N A:PRO700 4.5 2.2 1.0
C A:CYS699 4.5 2.5 1.0
SG A:CYS748 4.6 2.2 1.0
CG1 A:ILE704 4.6 2.0 1.0
N A:ALA703 4.7 2.1 1.0
CD1 A:ILE704 4.8 2.2 1.0
CA A:ALA703 4.8 2.3 1.0
SG A:CYS751 4.8 2.0 1.0
N A:HIS701 4.9 3.0 1.0
SG A:CYS745 4.9 2.1 1.0

Iron binding site 6 out of 24 in 1b0p

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Iron binding site 6 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 6 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1234

b:2.0
occ:1.00
FE2 A:SF41234 0.0 2.0 1.0
S4 A:SF41234 2.3 3.3 1.0
S1 A:SF41234 2.3 2.6 1.0
S3 A:SF41234 2.4 4.4 1.0
SG A:CYS745 2.4 2.1 1.0
FE3 A:SF41234 2.7 4.0 1.0
FE1 A:SF41234 2.7 3.8 1.0
FE4 A:SF41234 2.7 2.2 1.0
CB A:CYS745 3.5 2.0 1.0
CA A:CYS745 3.9 2.2 1.0
S2 A:SF41234 3.9 3.5 1.0
N A:MET746 3.9 2.7 1.0
CD A:PRO682 4.0 2.4 1.0
N A:GLY747 4.0 3.0 1.0
C A:CYS745 4.3 2.5 1.0
CB A:ALA703 4.5 2.3 1.0
CG A:PRO682 4.5 2.2 1.0
N A:CYS748 4.6 3.6 1.0
CA A:GLY747 4.6 3.0 1.0
SG A:CYS699 4.8 2.6 1.0
SG A:CYS751 4.8 2.0 1.0
C A:MET746 4.9 2.5 1.0
SG A:CYS748 4.9 2.2 1.0
CA A:MET746 5.0 2.5 1.0

Iron binding site 7 out of 24 in 1b0p

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Iron binding site 7 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 7 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1234

b:4.0
occ:1.00
FE3 A:SF41234 0.0 4.0 1.0
S2 A:SF41234 2.3 3.5 1.0
S1 A:SF41234 2.3 2.6 1.0
S4 A:SF41234 2.3 3.3 1.0
SG A:CYS751 2.3 2.0 1.0
FE2 A:SF41234 2.7 2.0 1.0
FE4 A:SF41234 2.7 2.2 1.0
FE1 A:SF41234 2.7 3.8 1.0
CB A:CYS751 3.4 2.9 1.0
S3 A:SF41234 3.9 4.4 1.0
N A:CYS751 4.0 2.0 1.0
CG A:PRO682 4.0 2.2 1.0
CD A:PRO682 4.2 2.4 1.0
CD1 A:ILE704 4.3 2.2 1.0
CA A:CYS751 4.3 2.0 1.0
SG A:CYS748 4.7 2.2 1.0
CG1 A:ILE704 4.7 2.0 1.0
SG A:CYS745 4.7 2.1 1.0
N A:GLY749 4.7 2.6 1.0
SG A:CYS699 4.7 2.6 1.0
CB A:PRO682 4.8 2.5 1.0
N A:ASN750 5.0 2.3 1.0

Iron binding site 8 out of 24 in 1b0p

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Iron binding site 8 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 8 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1234

b:2.2
occ:1.00
FE4 A:SF41234 0.0 2.2 1.0
S3 A:SF41234 2.3 4.4 1.0
S2 A:SF41234 2.3 3.5 1.0
SG A:CYS748 2.3 2.2 1.0
S1 A:SF41234 2.3 2.6 1.0
FE1 A:SF41234 2.6 3.8 1.0
FE3 A:SF41234 2.7 4.0 1.0
FE2 A:SF41234 2.7 2.0 1.0
CB A:CYS748 3.5 3.0 1.0
N A:CYS748 3.7 3.6 1.0
N A:GLY749 3.7 2.6 1.0
S4 A:SF41234 3.9 3.3 1.0
CA A:CYS748 4.0 3.0 1.0
CD A:PRO700 4.1 2.0 1.0
O A:HOH1349 4.2 2.0 1.0
C A:CYS748 4.3 2.4 1.0
N A:ASN750 4.4 2.3 1.0
SG A:CYS699 4.6 2.6 1.0
CA A:GLY749 4.7 2.8 1.0
SG A:CYS751 4.7 2.0 1.0
C A:GLY747 4.8 3.7 1.0
N A:GLY747 4.8 3.0 1.0
N A:CYS751 4.9 2.0 1.0
SG A:CYS745 4.9 2.1 1.0
C A:GLY749 4.9 2.6 1.0
CB A:ASN750 5.0 2.0 1.0
CG A:PRO700 5.0 2.0 1.0

Iron binding site 9 out of 24 in 1b0p

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Iron binding site 9 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 9 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1235

b:2.0
occ:1.00
FE1 A:SF41235 0.0 2.0 1.0
S2 A:SF41235 2.2 2.0 1.0
S3 A:SF41235 2.3 2.0 1.0
SG A:CYS812 2.3 2.1 1.0
S4 A:SF41235 2.4 2.0 1.0
FE4 A:SF41235 2.6 2.0 1.0
FE2 A:SF41235 2.7 2.2 1.0
FE3 A:SF41235 2.7 4.5 1.0
CB A:CYS812 3.3 2.0 1.0
S1 A:SF41235 3.9 2.6 1.0
N A:CYS812 3.9 2.0 1.0
CG1 A:ILE1072 3.9 2.1 1.0
CD1 A:ILE1072 4.2 2.0 1.0
CA A:CYS812 4.2 2.0 1.0
CD A:LYS459 4.5 3.0 1.0
SG A:CYS1071 4.6 2.0 1.0
SG A:CYS840 4.7 2.0 1.0
SG A:CYS815 4.7 2.0 1.0
NZ A:LYS459 4.8 2.8 1.0
CG2 A:ILE1072 4.8 2.0 1.0
CB A:CYS815 4.9 2.0 1.0
N A:ILE1072 4.9 2.4 1.0
CB A:ILE1072 4.9 2.2 1.0

Iron binding site 10 out of 24 in 1b0p

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Iron binding site 10 out of 24 in the Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 10 of Crystal Structure of Pyruvate-Ferredoxin Oxidoreductase From Desulfovibrio Africanus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1235

b:2.2
occ:1.00
FE2 A:SF41235 0.0 2.2 1.0
S4 A:SF41235 2.3 2.0 1.0
S1 A:SF41235 2.3 2.6 1.0
SG A:CYS815 2.3 2.0 1.0
S3 A:SF41235 2.3 2.0 1.0
FE3 A:SF41235 2.6 4.5 1.0
FE1 A:SF41235 2.7 2.0 1.0
FE4 A:SF41235 2.7 2.0 1.0
CB A:CYS815 3.3 2.0 1.0
S2 A:SF41235 3.9 2.0 1.0
CA A:CYS815 3.9 2.3 1.0
CG A:GLU817 4.4 2.1 1.0
N A:GLY816 4.4 2.0 1.0
C A:CYS815 4.6 2.0 1.0
N A:CYS812 4.6 2.0 1.0
CD A:GLU817 4.6 2.1 1.0
SG A:CYS812 4.6 2.1 1.0
SG A:CYS840 4.7 2.0 1.0
OE1 A:GLU817 4.7 2.4 1.0
SG A:CYS1071 4.8 2.0 1.0
CB A:CYS812 4.8 2.0 1.0
O A:THR1070 4.9 2.6 1.0
CB A:ALA811 5.0 2.0 1.0
CB A:GLU817 5.0 2.2 1.0
N A:GLU817 5.0 2.1 1.0

Reference:

E.Chabriere, M.H.Charon, A.Volbeda, L.Pieulle, E.C.Hatchikian, J.C.Fontecilla-Camps. Crystal Structures of the Key Anaerobic Enzyme Pyruvate:Ferredoxin Oxidoreductase, Free and in Complex with Pyruvate. Nat.Struct.Biol. V. 6 182 1999.
ISSN: ISSN 1072-8368
PubMed: 10048931
DOI: 10.1038/5870
Page generated: Wed Jul 16 12:19:58 2025

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